2,2'-Bipyridine (Highly Pure)
<strong>2,2'-Bipyridine (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2015390_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 50 g_x000D_ <strong>Molecular Weight or Concentration:</strong> 156.19 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8 °C_x000D_ <strong>Keywords:</strong> α,α’-Dipyridyl, BPY_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Constable EC, Housecroft CE. The Early Years of 2,2'-Bipyridine-A Ligand in Its Own Lifetime Molecules. 2019 Oct 31;24(21):3951._x000D_ 2: Chen D, Zhao Q, Liu W. Discovery of caerulomycin/collismycin-type 2,2'-bipyridine natural products in the genomic era J Ind Microbiol Biotechnol. 2019 Mar;46(3-4):459-468._x000D_ 3: Zhu Z, Wei L, Yadav AK, Fan Z, Kumar A, Miao M, Banerjee S, Huang H. Cyanine-Functionalized 2,2'-Bipyridine Compounds for Photocatalytic Cancer Therapy J Org Chem. 2023 Jan 6;88(1):626-631._x000D_ 4: Ievlev MY, Mayorov NS, Bardasov IN, Sorokin SP, Belikov MY, Ershov OV. Synthesis and Chemosensory Properties of New Cyanosubstituted 2,2'-Bipyridine Derivatives J Fluoresc. 2022 Nov;32(6):2333-2342._x000D_ 5: Wang L, Li T, Perveen S, Zhang S, Wang X, Ouyang Y, Li P. Nickel-Catalyzed Enantioconvergent Carboxylation Enabled by a Chiral 2,2'-Bipyridine Ligand Angew Chem Int Ed Engl. 2022 Dec 19;61(51):e202213943._x000D_ 6: Kruger PE. Coordination polymers and metal-organic frameworks derived from 4,4'-dicarboxy-2,2'-bipyridine and 4,4',6,6'-tetracarboxy-2,2'-bipyridine ligands: a personal perspective Chimia (Aarau). 2013;67(6):403-10._x000D_ 7: Puttaswamy NY, Mahanta P, Sarma P, Medhi C, Kaid SMA, Kullaiah B, Basumatary D, Manjasetty BA. Structure-based biological investigations on ruthenium complexes containing 2,2'-bipyridine ligands and their applications in photodynamic therapy as a potential photosensitizer Chem Biol Drug Des. 2023 Dec;102(6):1506-1520._x000D_ 8: Shenderovich IG. Weak, Broken, but Working-Intramolecular Hydrogen Bond in 2,2'-bipyridine Int J Mol Sci. 2023 Jun 20;24(12):10390._x000D_ 9: Kondori T, Akbarzadeh-T N, Ghaznavi H, Karimi Z, Shahraki J, Sheervalilou R, Shahraki O. A binuclear iron(III) complex of 5,5'-dimethyl-2,2'-bipyridine as cytotoxic agent Biometals. 2020 Dec;33(6):365-378._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/33866045">10: Smith GL, Reutovich AA, Srivastava AK, Reichard RE, Welsh CH, Melman A, Bou-Abdallah F. Complexation of ferrous ions by ferrozine, 2,2'-bipyridine and 1,10-phenanthroline: Implication for the quantification of iron in biological systems J Inorg Biochem. 2021 Jul;220:111460. </a>_x000D_ _x000D_ <strong>Products Related to 2,2'-Bipyridine (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>
Product Specifications
Short Description
Catalog Number: B2015390 (50 g)
Weight
2.6
Length
3.3
Width
1.2
Height
1.2
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